Canonical Allele Identifier: PA298827
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182330
ClinVar RCV Id: RCV000160319 RCV000212323 RCV000477092 RCV000663309 RCV000781178 RCV001194708 RCV003315951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys797Arg
CA298825
NM_032043.3:c.2390A>G